Primary Device ID | 20643169060832 |
NIH Device Record Key | b6bf124a-1a87-408a-b6e1-5834ced63a65 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TriVantage™ |
Version Model Number | 8229736 |
Company DUNS | 835465063 |
Company Name | MEDTRONIC XOMED, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Outer Diameter | 8.2 Millimeter |
Outer Diameter | 8.2 Millimeter |
Outer Diameter | 8.2 Millimeter |
Outer Diameter | 8.2 Millimeter |
Lumen/Inner Diameter | 6 Millimeter |
Outer Diameter | 8.2 Millimeter |
Lumen/Inner Diameter | 6 Millimeter |
Outer Diameter | 8.2 Millimeter |
Lumen/Inner Diameter | 6 Millimeter |
Outer Diameter | 8.2 Millimeter |
Lumen/Inner Diameter | 6 Millimeter |
Outer Diameter | 8.2 Millimeter |
Lumen/Inner Diameter | 6 Millimeter |
Outer Diameter | 8.2 Millimeter |
Lumen/Inner Diameter | 6 Millimeter |
Outer Diameter | 8.2 Millimeter |
Lumen/Inner Diameter | 6 Millimeter |
Outer Diameter | 8.2 Millimeter |
Lumen/Inner Diameter | 6 Millimeter |
Outer Diameter | 8.2 Millimeter |
Lumen/Inner Diameter | 6 Millimeter |
Outer Diameter | 8.2 Millimeter |
Lumen/Inner Diameter | 6 Millimeter |
Outer Diameter | 8.2 Millimeter |
Lumen/Inner Diameter | 6 Millimeter |
Outer Diameter | 8.2 Millimeter |
Lumen/Inner Diameter | 6 Millimeter |
Outer Diameter | 8.2 Millimeter |
Lumen/Inner Diameter | 6 Millimeter |
Outer Diameter | 8.2 Millimeter |
Lumen/Inner Diameter | 6 Millimeter |
Outer Diameter | 8.2 Millimeter |
Lumen/Inner Diameter | 6 Millimeter |
Outer Diameter | 8.2 Millimeter |
Lumen/Inner Diameter | 6 Millimeter |
Outer Diameter | 8.2 Millimeter |
Lumen/Inner Diameter | 6 Millimeter |
Outer Diameter | 8.2 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00643169060838 [Primary] |
GS1 | 20643169060832 [Package] Contains: 00643169060838 Package: PK [3 Units] In Commercial Distribution |
ETN | STIMULATOR, NERVE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-04-22 |
20643169060863 | EMG TUBE 8229739 3PK NIM TRIVANTAGE 9MM |
20643169060856 | EMG TUBE 8229738 3PK NIM TRIVANTAGE 8MM |
20643169060849 | EMG TUBE 8229737 3PK NIM TRIVANTAGE 7MM |
20643169060832 | EMG TUBE 8229736 3PK NIM TRIVANTAGE 6MM |
20643169060825 | EMG TUBE 8229735 3PK NIM TRIVANTAGE 5MM |